Journal: Hemoglobin - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Journal Hemoglobin

1. Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses. (2nd January 2016)

Authors:: Surapolchai, Pacharapan; Sirachainan, Nongnuch; So, Chi-Chiu; Hongeng, Suradej; Pakakasama, Samart; Anurathapan, Usanarat; Chuansumrit, Ampaiwan
Journal:: Hemoglobin
Issue:: Volume 40:Number 1(2016)
Page Start:: 70
Record Type:: Journal Article
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2. A Further Note on the Thalassemia Screening Program in the Muğla Region of Turkey. (2nd January 2016)

Authors:: Akar, Nejat
Journal:: Hemoglobin
Issue:: Volume 40:Number 1(2016)
Page Start:: 74
Record Type:: Journal Article
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3. Insights into the Progression of Labile Hb A1c to Stable Hb A1cvia a Mechanistic Assessment of 2, 3-Bisphosphoglycerate Facilitation of the Slow Nonenzymatic Glycation Process. (2nd January 2019)

Authors:: Mottishaw, Christina R.; Becker, Stephanie; Smith, Brandy; Titus, Gentry; Holman, R.W.; Rodnick, Kenneth J.
Journal:: Hemoglobin
Issue:: Volume 43:Number 1(2019)
Page Start:: 42
Record Type:: Journal Article
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4. Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous α-Thalassemia-2. (2nd January 2019)

Authors:: Nuinoon, Manit; Thipthara, Orapan; Fucharoen, Suthat
Journal:: Hemoglobin
Issue:: Volume 43:Number 1(2019)
Page Start:: 52
Record Type:: Journal Article
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5. Severe Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln; HBB: c.442T>C)] on the β-Globin Gene. (2nd January 2019)

Authors:: Su, Qiong; Chen, Shiping; Wu, Liusong; Tian, Runmei; Yang, Xiaoqin; Huang, Xiaoyan; Chen, Yan; Peng, Zhiyu; Chen, Jindong
Journal:: Hemoglobin
Issue:: Volume 43:Number 1(2019)
Page Start:: 7
Record Type:: Journal Article
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6. Purulent Pericarditis in Sickle Cell Disease Due to Streptococcus agalactiae; a Unique Case Report and Literature Review. (2nd January 2019)

Authors:: Bhat, Alina; Neculiseanu, Elvira; Tam, Eric L.; Gendy, Adam; Beckles, Daniel L.; Luhrs, Carol; Braverman, Albert
Journal:: Hemoglobin
Issue:: Volume 43:Number 1(2019)
Page Start:: 1
Record Type:: Journal Article
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7. First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family. (2nd January 2019)

Authors:: Murad, Hossam; Moassas, Faten
Journal:: Hemoglobin
Issue:: Volume 43:Number 1(2019)
Page Start:: 66
Record Type:: Journal Article
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8. The Spectrum of β-Thalassemia Mutations in Hamadan Province, West Iran. (2nd January 2019)

Authors:: Alibakhshi, Reza; Moradi, Keivan; Aznab, Mozaffar; Azimi, Azam; Shafieenia, Samaneh; Biglari, Mostafa
Journal:: Hemoglobin
Issue:: Volume 43:Number 1(2019)
Page Start:: 18
Record Type:: Journal Article
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9. Hb Milano [α109(G16)Leu→Pro (CTG>CCG); HBA1: c.329T>C]: A Novel Variant on the α1-Globin Gene in an Italian Family. (2nd January 2019)

Authors:: Curcio, Cristina; Giannone, Valentina; Benzoni, Elena; Cesaretti, Claudia; Ivaldi, Giovanni
Journal:: Hemoglobin
Issue:: Volume 43:Number 1(2019)
Page Start:: 4
Record Type:: Journal Article
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10. A Case Report of Compound Heterozygosity for β0/β+-Thalassemia Resulting from under Diagnosed β-Thalassemia Found in a Hb A'2 Sample. (2nd January 2019)

Authors:: Intasai, Nutjeera; Phasit, Ampai; Panyasai, Sitthichai; Pornprasert, Sakorn
Journal:: Hemoglobin
Issue:: Volume 43:Number 1(2019)
Page Start:: 63
Record Type:: Journal Article
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